New Fusarochromanone Derivatives from the Marine Fungus Fusarium equiseti UBOCC-A-117302
Abstract
:1. Introduction
2. Results and Discussion
2.1. FBMN Analysis and Metabolite Annotation
2.2. Structure Elucidation
2.3. Biological Assays
3. Materials and Methods
3.1. General Experimental Procedure
3.2. Isolation and Identification of the Fungus
3.3. Fermentation
3.4. Global Natural Products Social Molecular Networking
3.5. Extraction and Purification
3.6. Kinase Inhibition Assays
3.7. Cytotoxic Assay
3.7.1. Cell Culture
3.7.2. Cell Viability
3.8. Antimicrobial Assay
4. Conclusions
Supplementary Materials
Author Contributions
Funding
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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Position | 1 | 2 | ||
---|---|---|---|---|
1H [δ, mult. (J in Hz)] | 13C (δ) | 1H [δ, mult. (J in Hz)] | 13C (δ) | |
2 | - | 77.6 | - | 77.5 |
3 | 5.65 d (10.0) | 128.9 | 5.64 d (10.0) | 128.8 |
4 | 6.58 d (10.0) | 117.1 | 6.59 d (10.0) | 117.3 |
5 | - | 150.2 | - | 150.6 |
6 | - | 112.8 | - | 113.9 |
7 | 7.61 d (9.0) | 133.9 | 7.70 d (9.0) | 134.5 |
8 | 6.12 d (9.0) | 106.9 | 6.11 d (9.0) | 106.6 |
9 | - | 159.9 | - | 159.7 |
10 | - | 107.6 | - | 107.6 |
11 | 1.40 s | 28.0 | 1.40 s | 28.0 |
12 | 1.40 s | 28.0 | 1.41 s | 28.0 |
1′ | - | 198.0 | - | 192.2 |
2′ | 3.36 m 3.21 dd (18.0, 8.3) | 38.5 | 7.23 dt (15.2, 2.0) | 126.1 |
3′ | 3.77 m | 51.2 | 6.90 dt (15.2, 4.1) | 145.6 |
4′ | 3.82 m 3.67 dd (10.7, 5.5) | 62.7 | 4.33 dd (4.1, 2.2) | 62.6 |
Compound | EC50 (µM) | ||
---|---|---|---|
RPE-1 | HCT-116 | U2OS | |
1 | 0.176 | 0.087 | 0.896 |
2 | 10.030 | 13.730 | 13.180 |
3 | 23.140 | 62.950 | 35.090 |
4 | 16.700 | 84.380 | 39.790 |
5 | 5.222 | 8.036 | 7.351 |
6 | 0.058 | 0.170 | 0.232 |
7 | >25 | >25 | >25 |
8 | >25 | >25 | >25 |
Staurosporine | 1.900 | 25.700 | 9.900 |
MBC/MIC (µM) | ||||
---|---|---|---|---|
Compound | 2 | 4 | 8 | Erythromycin |
L. monocytogenes SOR 100 | 125* | 125 * | 31.25 ** | 1.36 |
E. faecalis CIP A 186 | (−) | (−) | 31.25 * | 5.44 |
B. cereus ATCC 6464 | (−) | (−) | 7.8 ** | 5.45 |
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Pham, G.N.; Josselin, B.; Cousseau, A.; Baratte, B.; Dayras, M.; Le Meur, C.; Debaets, S.; Weill, A.; Robert, T.; Burgaud, G.; et al. New Fusarochromanone Derivatives from the Marine Fungus Fusarium equiseti UBOCC-A-117302. Mar. Drugs 2024, 22, 444. https://doi.org/10.3390/md22100444
Pham GN, Josselin B, Cousseau A, Baratte B, Dayras M, Le Meur C, Debaets S, Weill A, Robert T, Burgaud G, et al. New Fusarochromanone Derivatives from the Marine Fungus Fusarium equiseti UBOCC-A-117302. Marine Drugs. 2024; 22(10):444. https://doi.org/10.3390/md22100444
Chicago/Turabian StylePham, Giang Nam, Béatrice Josselin, Arnaud Cousseau, Blandine Baratte, Marie Dayras, Christophe Le Meur, Stella Debaets, Amélie Weill, Thomas Robert, Gaëtan Burgaud, and et al. 2024. "New Fusarochromanone Derivatives from the Marine Fungus Fusarium equiseti UBOCC-A-117302" Marine Drugs 22, no. 10: 444. https://doi.org/10.3390/md22100444
APA StylePham, G. N., Josselin, B., Cousseau, A., Baratte, B., Dayras, M., Le Meur, C., Debaets, S., Weill, A., Robert, T., Burgaud, G., Probert, I., Abdoul-Latif, F. M., Boyer, L., Bach, S., & Mehiri, M. (2024). New Fusarochromanone Derivatives from the Marine Fungus Fusarium equiseti UBOCC-A-117302. Marine Drugs, 22(10), 444. https://doi.org/10.3390/md22100444